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Quality

Agile Pharma’s quality system is based on Good Manufacturing Practices GMP I and II IC HQ7 for Active Pharmaceutical Ingredients (API’s).

We supply state of the art quality and wherever possible continuously improve the quality of our products and services. In order to be able to achieve these goals, Agile Pharma invests in well trained personnel, as well as in the availability of suitable equipment and infrastructure. We consider keeping the knowledge and skills of personnel up to date of major importance, and therefore offer the possibilities for the employees to take part in training programs.

Agile Pharma is periodically inspected by the Ministry of Health. In addition, periodic internal audits are conducted to verify the internal procedures and to work on continuous improvement of our procedures.
Customers are welcome to carry out on site audits at our premises.

All our suppliers and contractors are qualified by means of audits or extensive questionnaires in order to make sure they comply to the same set of quality standards.

Agile Pharma holds the following certificates and licences:

  • A GMP license for sampling and re-packaging of pharmaceutical raw materials, in accordance with the EU directives on GMP (Good Manufacturing Practice).
  • A GDP (Good Distribution Practice) license for the distribution and storage of pharmaceutical raw materials in our warehouse.
  • An API (Active Pharmaceutical Ingredient) registration for both human and veterinary products
  • A controlled drug license
  • A License for Precursors